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Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis

The early development of many animals relies on the posttranscriptional regulations of maternally stored mRNAs. In particular, the translation of maternal mRNAs is tightly controlled during oocyte maturation and early mitotic cycles in Xenopus. The Embryonic Deadenylation ElemeNt (EDEN) and its asso...

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Autores principales: Graindorge, Antoine, Le Tonquèze, Olivier, Thuret, Raphaël, Pollet, Nicolas, Osborne, H. Beverley, Audic, Yann
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330240/
https://www.ncbi.nlm.nih.gov/pubmed/18267972
http://dx.doi.org/10.1093/nar/gkn031
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author Graindorge, Antoine
Le Tonquèze, Olivier
Thuret, Raphaël
Pollet, Nicolas
Osborne, H. Beverley
Audic, Yann
author_facet Graindorge, Antoine
Le Tonquèze, Olivier
Thuret, Raphaël
Pollet, Nicolas
Osborne, H. Beverley
Audic, Yann
author_sort Graindorge, Antoine
collection PubMed
description The early development of many animals relies on the posttranscriptional regulations of maternally stored mRNAs. In particular, the translation of maternal mRNAs is tightly controlled during oocyte maturation and early mitotic cycles in Xenopus. The Embryonic Deadenylation ElemeNt (EDEN) and its associated protein EDEN-BP are known to trigger deadenylation and translational silencing to several mRNAs bearing an EDEN. This Xenopus RNA-binding protein is an ortholog of the human protein CUG-BP1/CELF1. Five mRNAs, encoding cell cycle regulators and a protein involved in the notch pathway, have been identified as being deadenylated by EDEN/EDEN-BP. To identify new EDEN-BP targets, we immunoprecipitated EDEN-BP/mRNA complexes from Xenopus tropicalis egg extracts. We identified 153 mRNAs as new binding targets for EDEN-BP using microarrays. Sequence analyses of the 3′ untranslated regions of the newly identified EDEN-BP targets reveal an enrichment in putative EDEN sequences. EDEN-BP binding to a subset of the targets was confirmed both in vitro and in vivo. Among the newly identified targets, Cdk1, a key player of oocyte maturation and cell cycle progression, is specifically targeted by its 3′ UTR for an EDEN-BP-dependent deadenylation after fertilization.
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spelling pubmed-23302402008-05-05 Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis Graindorge, Antoine Le Tonquèze, Olivier Thuret, Raphaël Pollet, Nicolas Osborne, H. Beverley Audic, Yann Nucleic Acids Res Molecular Biology The early development of many animals relies on the posttranscriptional regulations of maternally stored mRNAs. In particular, the translation of maternal mRNAs is tightly controlled during oocyte maturation and early mitotic cycles in Xenopus. The Embryonic Deadenylation ElemeNt (EDEN) and its associated protein EDEN-BP are known to trigger deadenylation and translational silencing to several mRNAs bearing an EDEN. This Xenopus RNA-binding protein is an ortholog of the human protein CUG-BP1/CELF1. Five mRNAs, encoding cell cycle regulators and a protein involved in the notch pathway, have been identified as being deadenylated by EDEN/EDEN-BP. To identify new EDEN-BP targets, we immunoprecipitated EDEN-BP/mRNA complexes from Xenopus tropicalis egg extracts. We identified 153 mRNAs as new binding targets for EDEN-BP using microarrays. Sequence analyses of the 3′ untranslated regions of the newly identified EDEN-BP targets reveal an enrichment in putative EDEN sequences. EDEN-BP binding to a subset of the targets was confirmed both in vitro and in vivo. Among the newly identified targets, Cdk1, a key player of oocyte maturation and cell cycle progression, is specifically targeted by its 3′ UTR for an EDEN-BP-dependent deadenylation after fertilization. Oxford University Press 2008-04 2008-02-11 /pmc/articles/PMC2330240/ /pubmed/18267972 http://dx.doi.org/10.1093/nar/gkn031 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Graindorge, Antoine
Le Tonquèze, Olivier
Thuret, Raphaël
Pollet, Nicolas
Osborne, H. Beverley
Audic, Yann
Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title_full Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title_fullStr Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title_full_unstemmed Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title_short Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis
title_sort identification of cug-bp1/eden-bp target mrnas in xenopus tropicalis
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330240/
https://www.ncbi.nlm.nih.gov/pubmed/18267972
http://dx.doi.org/10.1093/nar/gkn031
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